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Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Place a burning splint near the opening of a test tube. If a popping noise occurs, it's probably hydrogen. Place a glowing splint in the test tube, and if it reignites, it could be oxygen. Place a burning splint into a test tube, and if it goes out, it could be carbon dioxide.
